Common questions

What is paroxysmal nocturnal hemoglobinuria (PNH)?

PNH is a rare blood disease that causes below-normal levels of hemoglobin, a protein in red blood cells that is responsible for moving oxygen around the body.

What causes PNH?

PNH is caused by a genetic mutation. This change in the body’s DNA causes red blood cells to be produced without key proteins needed to protect them from the body’s immune systemimmune systemA sophisticated defense network used to protect the body from dangers like disease and infection.. Without this shield, the immune system attacks them.

What is hemolysis?

Hemolysis refers to the “breaking apart” of red blood cells. It occurs when the immune system attacks these cells as though they were dangerous viruses or bacteria. When red blood cells break open, hemoglobin is released. Hemolysis causes many of the symptoms of PNH.

What are the symptoms of PNH?

PNH symptoms vary from person to person. In some individuals they can be mild, in others more severe. Potential symptoms include:

  • FatiguefatigueExtreme tiredness or exhaustion. Fatigue is one of the most common symptoms of PNH.
  • Difficulty breathing
  • Bruising or bleeding easily
  • Small red dots on the skin
  • Severe headache
  • Blood clots
  • Blood in urine

How is PNH diagnosed?

PNH can be diagnosed through a wide range of blood tests. One of the most common methods is flow cytometryflow cytometryThe most common method of testing for PNH, this test confirms whether red blood cells are missing their protective shield. It also calculates the percentage of blood cells impacted by PNH, which is referred to as your clone size. A large clone size means you have a high percentage of blood cells that can be attacked by the complement system, which may lead to more severe symptoms., which can determine if there are proteinsproteinsLarge, complex molecules that play many important roles in the body and can be thought of as the “workhorses” of cells. Proteins are required for the structure, function and regulation of the body’s organs and tissues. missing from the surface of blood cells.

How many people have PNH?

Approximately 400-500 people are diagnosed with PNH in the United States every year. There may be as many as 5,000-6,000 people in the U.S. who have PNH.

Is PNH more common in a specific gender or race?

PNH can impact people of any age, gender or race. Most often, people are diagnosed during their 30s.

What are the risk factors for PNH?

The only known risk factor for PNH is aplastic anemia, a rare disease that occurs when a person’s bone marrowbone marrowThe soft fatty tissue inside certain bones that houses stem cells, some of which will ultimately become blood cells. Bone marrow provides the nutrients and environment needed for blood cells to be created. Once these cells are fully mature and ready to go to work, they leave the bone marrow and enter the bloodstream. does not make enough new blood cells. Some scientists believe that aplastic anemiaaplastic anemiaA rare blood disease that is a known risk factor for PNH. Aplastic anemia occurs when a person’s bone marrow does not make enough new blood cells. Some scientists believe that aplastic anemia weakens the body’s bone marrow, which then affects its ability to produce healthy red blood cells. weakens the body’s bone marrow, which then affects its ability to produce healthy red blood cells.

Is PNH a type of cancer?

PNH is not cancer. PNH is a rare blood disease. Blood cells originate in bone marrow. Other diseases involving bone marrow can be cancer (e.g., leukemia), but PNH is not one of them. Doctors who specialize in treating PNH often also treat people with cancer or work at centers that focus on treating people with cancer, but PNH should not be confused with cancer.

Will PNH impact my life expectancy?

PNH is not always life-threatening. Since the introduction of PNH treatments more than a decade ago, most people with PNH who do not develop additional complications have a relatively normal life expectancy. However, people can still be at risk for the development of blood clots or other disorders associated with PNH.

How does PNH impact daily life?

The daily reality of PNH is different for everyone. Some individuals have mild symptoms, while others have more severe symptoms. One of the most common experiences is fatigue that can impact how you spend time with others, complete daily tasks and pursue work-related activities.

Can I have children?

You may be able to have children. Women who are pregnant and have PNH have a higher risk of blood clots. If you are planning a family, you should speak with your doctor to determine if it’s safe. If you and your doctor decide a pregnancy is safe for you, you can work together to develop a plan to help prevent complications and minimize risk. This may include additional treatments.

What can I expect regarding fatigue?

Everyone’s experience with fatigue is different. Fatigue is often the most debilitating symptom impacting daily life and can feel worse than any lab test result might suggest. However, everyone’s experience is unique, and the same person can have different symptoms at different times. While some have symptoms that are mild and manageable, others may have symptoms that are more severe.

Can I pass this on to others?

PNH is not inherited and can’t be passed on to others. PNH is “acquired,” which means the genetic mutations responsible for the disease happen during your life. You are not born with them, and you cannot pass them on to others.

How can I connect with other members of the PNH community?

AAMDSIF is a resource that hosts local events and a Peer Support Network.

Apellis also offers opportunities to connect via:

Where can I go for information about PNH?

Your healthcare provider is always the best place to turn for information about your condition and how best to treat it. A full list of additional supportive resources can be found here.

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